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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25278Generated: October 26, 2026

Water → 2-Cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile

https://huagongshe.com/reaction/25278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(Bromomethyl)cyclobutaneHCID 2734658—
ReactantHCID 178509603HCID 178509603—
SolventDimethylformamideHCID 6228—
Product2-Cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrileHCID 17850960521.6%

Reaction Steps

0.9 g (3.3 mmol) of 2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile, 0.5 g (3.3 mmol) of cyclobutylmethyl bromide and 0.55 g (4.0 mmol) of potassium carbonate were stirred in 5 ml of N,N-dimethylformamide at room temperature overnight. The resulting reaction mixture was poured into 50 ml of water and the organic matters were extracted with 20 ml of ethyl acetate twice. The ethyl acetate layers were combined, then washed with 30 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 0.24 g of 2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 21.2%) as a pale yellow powder (m.p. 102-103° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858639B2
Source datasetuspto-grants-2005_02
ORD IDord-109991864653475a9fb514957c60a928
Source noteuspto-grants-2005_02